← FDA Drug Approvals (Drugs@FDA)
TENUATE
NDA · New Drug Application · Sponsor: SANOFI AVENTIS US · Approved 1975-03-20
Drug application
- FDA Application #
NDA017669- Application type
- New Drug Application
- Brand name
- TENUATE
- Generic name
- Diethylpropion Hydrochloride
- Active ingredients
- DIETHYLPROPION HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- SANOFI AVENTIS US
- First approval
- 1975-03-20
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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